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Found 7 results
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2013
Dury AY, Fatimy REl, Tremblay S, Rose TM, Côté J, De Koninck P, Khandjian EW
. 2013.
Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.
.
PLoS Genet. 9(10):e1003890.
2012
Flynn R, Labrie-Dion É, Bernier N, Colicos MA, De Koninck P, Zamponi GW
. 2012.
Activity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIα.
.
PLoS One. 7(7):e41185.
Fatimy REl, Tremblay S, Dury AY, Solomon S, De Koninck P, Schrader JW, Khandjian EW
. 2012.
Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].
.
PLoS One. 7(6):e39338.
2006
Davidovic L, Tremblay S, Gravel M, De Koninck P, Khandjian EWMiky
. 2006.
[The fragile X syndrome: one protein missing and 1001 disoriented mRNAs].
.
Med Sci (Paris). 22(1):41-6.
Bayer K U, Lebel E, McDonald GL, O'Leary H, Schulman H, De Koninck P
. 2006.
Transition from reversible to persistent binding of CaMKII to postsynaptic sites and NR2B.
.
J Neurosci. 26(4):1164-74.
2005
Hudmon A, Lebel E, Roy H, Sik A, Schulman H, M Waxham N, De Koninck P
. 2005.
A mechanism for Ca2+/calmodulin-dependent protein kinase II clustering at synaptic and nonsynaptic sites based on self-association.
.
J Neurosci. 25(30):6971-83.
Costantino S, Heinze KG, Martínez OE, De Koninck P, Wiseman PW
. 2005.
Two-photon fluorescent microlithography for live-cell imaging.
.
Microsc Res Tech. 68(5):272-6.
Funding
Our research endeavors are made possible by the following agencies: